ZNF335

zinc finger protein 335

Summary

The protein encoded by this gene enhances transcriptional activation by ligand-bound nuclear hormone receptors. However, it does this not by direct interaction with the receptor, but by direct interaction with the nuclear hormone receptor transcriptional coactivator NRC. The encoded protein may function by altering local chromatin structure. [provided by RefSeq, Jul 2008]

Known Variants520 total

rsid	Position (GRCh37)	Alleles	Class	ClinVar
rs6130975	20:44,576,982	G/C	—	—
rs3363	20:44,577,314	T/C	—	likely benign
rs2145349695	20:44,577,595	G/A	—	likely benign
rs781092251	20:44,577,601	G/A	—	likely benign
rs372687838	20:44,577,615	C/T	—	uncertain significance
rs748843555	20:44,577,618	C/T	—	uncertain significance
rs199912926	20:44,577,620	T/C	—	uncertain significance
rs200635860	20:44,577,623	T/C	—	uncertain significance
rs139630946	20:44,577,630	C/T	—	uncertain significance
rs764029673	20:44,577,637	C/G	—	uncertain significance
rs2083575738	20:44,577,648	G/C	—	uncertain significance
rs767339054	20:44,577,657	C/T	—	uncertain significance
rs114581171	20:44,577,658	G/A	—	benign
rs142441368	20:44,577,669	C/T	—	uncertain significance
rs373702846	20:44,577,670	G/A	—	likely benign
rs2515520823	20:44,577,708	C/T	—	uncertain significance
rs1466554079	20:44,577,709	A/T	—	uncertain significance
rs2515520900	20:44,577,724	C/T	—	uncertain significance
rs760509101	20:44,577,802	T/G	—	likely benign
rs1279130921	20:44,577,822	G/T	—	uncertain significance
rs755337564	20:44,577,825	T/C	—	likely benign
rs1426731507	20:44,577,832	G/A	—	uncertain significance
rs770300456	20:44,577,842	G/A	—	likely benign
rs777764325	20:44,577,852	G/A	—	likely benign
rs35291173	20:44,577,867	T/C	—	conflicting classifications of pathogenicity
rs140528177	20:44,577,868	G/A	—	conflicting classifications of pathogenicity
rs765257687	20:44,577,870	G/A	—	likely benign
rs754608119	20:44,577,897	G/A	—	likely benign
rs191147826	20:44,577,901	G/A	—	likely benign
rs959893772	20:44,577,907	G/A	—	likely benign
rs778980849	20:44,577,966	C/T	—	uncertain significance
rs745927171	20:44,577,967	C/T	—	uncertain significance
rs1247865358	20:44,577,978	C/T	—	likely benign
rs2515522045	20:44,577,987	G/A	—	likely benign
rs113958814	20:44,577,991	G/T	—	likely benign
rs749190523	20:44,578,004	C/A	stop gained	pathogenic
rs1172684207	20:44,578,028	C/T	—	uncertain significance
rs760353441	20:44,578,034	G/C	—	uncertain significance
rs1254644501	20:44,578,041	C/T	—	likely benign
rs928931258	20:44,578,045	G/A	—	likely benign
rs1426100407	20:44,578,046	A/G	—	likely benign
rs41280270	20:44,578,050	A/G	—	likely benign
rs375133385	20:44,578,108	C/T	—	likely benign
rs2515522620	20:44,578,139	T/G	—	uncertain significance
rs569368236	20:44,578,155	T/A	—	uncertain significance
rs763575505	20:44,578,157	T/C	—	likely benign
rs755176005	20:44,578,163	G/A	—	likely benign
rs2515522733	20:44,578,166	G/A	—	likely benign
rs753015159	20:44,578,181	A/G	—	likely benign
rs1057520125	20:44,578,200	T/C	—	uncertain significance
rs902538647	20:44,578,202	C/T	—	uncertain significance
rs772015167	20:44,578,215	T/G	—	conflicting classifications of pathogenicity
rs376616764	20:44,578,218	G/T	—	likely benign
rs373445422	20:44,578,222	G/A	—	likely benign
rs1365216449	20:44,578,447	C/T	—	uncertain significance
rs747689204	20:44,578,448	G/A	—	likely benign
rs755637424	20:44,578,450	A/C	—	uncertain significance
rs2145352896	20:44,578,458	A/G	—	uncertain significance
rs774881765	20:44,578,468	C/T	—	uncertain significance
rs191074858	20:44,578,469	G/A	—	conflicting classifications of pathogenicity
rs1191013997	20:44,578,492	T/C	—	uncertain significance
rs138802024	20:44,578,508	G/A	—	likely benign
rs41280272	20:44,578,530	A/G	—	benign
rs201495017	20:44,578,549	C/G	—	likely benign
rs1600517442	20:44,578,607	G/A	—	uncertain significance
rs148934939	20:44,578,635	G/A	—	likely benign
rs373788531	20:44,578,669	C/T	—	uncertain significance
rs2083600323	20:44,578,671	C/T	—	likely benign
rs16990951	20:44,578,674	T/A	—	benign
rs764681680	20:44,578,679	C/A	—	uncertain significance
rs1427279281	20:44,578,688	C/T	—	uncertain significance
rs141812371	20:44,578,689	G/A	—	likely benign
rs755393287	20:44,578,703	G/A	—	uncertain significance
rs116077790	20:44,578,707	A/G	—	likely benign
rs201983124	20:44,578,714	C/T	—	likely benign
rs966132762	20:44,578,721	G/A	—	likely benign
rs771065323	20:44,578,723	G/A	—	likely benign
rs6065910	20:44,578,776	A/G	—	benign
rs115628563	20:44,578,812	C/G	—	likely benign
rs73622634	20:44,578,844	C/G	—	benign
rs768535357	20:44,578,864	G/A	—	likely benign
rs769608235	20:44,578,877	T/C	—	likely benign
rs142739306	20:44,578,880	G/A	—	benign
rs2083605557	20:44,578,889	G/A	—	likely benign
rs2515525367	20:44,578,892	C/G	—	likely benign
rs143113106	20:44,578,900	T/C	—	conflicting classifications of pathogenicity
rs759216909	20:44,578,901	G/A	—	conflicting classifications of pathogenicity
rs779169316	20:44,578,929	C/T	—	uncertain significance
rs200221426	20:44,578,930	G/A	—	uncertain significance
rs2515525519	20:44,578,933	C/T	—	uncertain significance
rs114864530	20:44,578,953	C/T	—	conflicting classifications of pathogenicity
rs770306876	20:44,578,956	C/G	—	uncertain significance
rs3746503	20:44,578,961	G/A	—	benign
rs775187200	20:44,578,964	A/G	—	likely benign
rs1055761936	20:44,578,979	G/C	—	uncertain significance
rs35156034	20:44,578,991	G/A	—	benign
rs754414245	20:44,578,994	G/T	—	uncertain significance
rs1278977251	20:44,578,997	C/T	—	likely benign
rs780393773	20:44,578,999	C/T	—	conflicting classifications of pathogenicity
rs779084748	20:44,579,016	A/G	—	likely benign

Showing 100 of 520 variants. Use the SNP search for the full list.

Gene information from NCBI Gene. Variant classifications from ClinVar.